Children Fighting Opsoclonus-Myoclonus Syndrome & Neuroblastoma

[TheZekeiscool]

im zeke and I'm the boy on the quad I'm 11 years old now still in remission

[1997natisha]

my daughter is dealing with oms. i blame the MMR. she had the jab at 13 months and at 18 months she started to get the same symptoms but no tuma, to meny test for her little body to cope with but she had no choice , after 6 months we had a diaognoies and she was put on steroids untill she was 8. i live in london and have never met a perant going thro the same heatake, this is ablessing seeing this on you tube and i would love to talk to some who know wot i have been thru with my little angel,

[DocSolomon]

@1997natisha u blame MMR... im sorry but that's just wrong

[1997natisha]

my daughter is dealing with oms. i blame the MMR. she had the jab at 13 months and at 18 months she started to get the same symptoms but no tuma, to meny test for her little body to cope with but she had no choice , after 6 months we had a diaognoies and she was put on steroids untill she was 8. i live in london and have never met a perant going thro the same heatake, this is ablessing seeing this on you tube and i would love to talk to some who know wot i have been thro with my little angel,

[anastasiapopovic]

hi,

very nice.My anastasia (now 7 years old) fighting oms from the 2006.

God bless all thoes children and their parents and give the faith.

[tarawoodman30]

yes my little boy is in this video

[tarawoodman30]

You asked how you could contact me I am on Facebook under Tara Woodman

[noonoo2345]

just want to say a mahoooosive thanx to u who made this video, it has really helped my friends and family understand my elsie's condition a whole lot more,

my daughter elsie has been fighting oms for a year and half now, she appears in this video,

to all the children out there that are fighting this condition u are all lil angels!!!!

mom of elsie x x x

[jeremie1104]

Bravo pour ce vidéo. Ma fille de 21 mois a eu le diagnostic OMS. C'est très difficile et j'ai énormément de peine de voir ma fille ainsi. Mais je reste positive.

[miniworld78]

Today, I visited my friend's baby boy in Childrens Hospital in Morris Town, NJ. And heard that he has OMS.

I did not know what it was... and now I know... And my friend does not... yet...

I really do not know what to say... but pray.

The deciples have done awsome workd in the name of Jesus Christ.

I believe God hears us.

God bless all thoes children and their parents.

[gdogw2]

Hi, I would love to share our story and add my son to the video if possible. It was so touching to watch. Great Job. I posted it to my facebook page for awareness. How can I get in touch with you? Thank you.

[tarawoodman30]

@gdogw2

I am on facebook under Tara Woodman in pa you could look me up that way

[bayleybrown]

tara thanks, It has been a year with oms for us and once in awhile I watch your video and know that we are not alone in this battle.

Julie Thomas

mom to Walter in the video

[yapcj]

Hi,

Thanks for the video clip.

It is hard to say this... but Thank God for OMS. Because of the symptoms, only then, we discovered (or rather, the doctors diagnosed) our daughter's neuroblastoma when she was 1 year old.

They are truly, beautiful creations of God whom He has put into the lives of the parents. They are the good and perfect gift from above (though the world may think otherwise, or may classify them as "defective"). But through them, we are made stronger... in faith.

God Bless.